Informed Consent Template (English Language) - UCLA :知情同意的模板(英文)-加州大学洛杉矶分校.doc,NCI-UCLA CONSENT FORM TEMPLATE Template Instructions: Instructions and examples for informed consent authors are in [italics]. A blank line, ___, i
临床研究申请书模版:informed_consent_template.docx,Version 2 – March 25, 2014 Page PAGE 9 of NUMPAGES 14 The below template for developing an informed consent document to use in your research study is meant to provide structure and guidance to the proce
B. The Informed Consent Process Informed consent is more than a form, it is also a process. Information must be presented to enable persons to voluntarily decide whether or not to participate as a research subject. Informed consent process must be a dialogue of the study’s purpose, duration...
(VA,FDA,PHS)Sponsor’sICFmaydifferUCHCtemplaterequiredelementsacceptablelanguage10ICFRequiredElementsBasicresearch,purposes,expecteddurationproceduresfollowed,experimentalproceduresReasonablyforeseeablerisksalternativeproceduressubjectrecordsmorethanminimalriskwhetheranytreatmentsavailableinjuryoccursanswerquestionsreresearchsubjects'...
InformedConsentForm(ICF)Essentials Formattingdocument:•••••1”marginforstamps&scanningFontsize–12,easilyreadablefontClearsectionheadingsSufficientwhitespaceUtilizationoftables/charts/picturestocommunicateapoint•Versionnumberinthefooter(changewhenrevised)6 ICFEssentials •CompleteICF:–PI,PIPhoneNumber...
Informed Consent Form (ICF) - Human Subjects :知情同意书(ICF)-人.ppt,Informed Consent Form (ICF) Health Insurance Portability and Accountability Act (HIPAA) Human Subject Protection Office UConn Health Center Monika Haugstetter, MHA, RN, MSN HSPO Webs
Informed Consent Form (ICF) - Human Subjects :知情同意书(ICF)-人书,人,帮助,ICF,Form,知情同意书,human,form,同意,Icf 文档格式: .ppt 文档大小: 53.5K 文档页数: 21页 顶/踩数: 0/0 收藏人数: 1 评论次数: 0 文档热度: 文档分类:
B. The Informed Consent Process Informed consent is more than a form, it is also a process. Information must be presented to enable persons to voluntarily decide whether or not to participate as a research subject. Informed consent process must be a dialogue of the study’s purpose, duration...
InformedConsentForm(ICF)Essentials Formattingdocument:•••••1”marginforstamps&scanningFontsize–12,easilyreadablefontClearsectionheadingsSufficientwhitespaceUtilizationoftables/charts/picturestocommunicateapoint•Versionnumberinthefooter(changewhenrevised)6 ICFEssentials •CompleteICF:–PI,PIPhoneNumber...
Thus, all needs for paper document, e.g., informed consent, transmission, subsequent storage, geographic proximity and/or travel are eliminated. Traditionally, the first step in assigning an electronic signature for clinical research that will undergo the FDA approval has been a paper-based ...